نتایج جستجو برای: genetic mutation

تعداد نتایج: 825720  

Journal: :ADI International Conference Series 2022

The problem of teacher placement in a school is faced by Magelang Regency. success determined the minimum total distance between and school, with aim that performance maintained. In computer science this an NP-hard takes very long time to achieve optimal results when done conventional methods. Another approach solve use heuristic algorithms, one which using genetic algorithms. To further improv...

Journal: :Lontar Komputer 2022

Heart disease is a leading cause of death worldwide, and the need for effective predictive systems major source to treat affected patients. This study aimed determine how improve accuracy Random Forest in predicting classifying heart disease. The experiments performed this were designed select most optimal parameters using an RF optimization technique GA. Genetic Algorithm (GA) used optimize pr...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه پیام نور - دانشگاه پیام نور استان تهران - دانشگاه پیام نور مرکز تهران - دانشکده علوم پایه 1387

چکیده ندارد.

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه اصفهان - دانشکده علوم 1388

چکیده ندارد.

Journal: :iranian biomedical journal 0
ایثار نصیری issar nassiri مهری فقیهی mehri faghihi منوچهر توسلی manoochehr tavassoli

background: pharmacogenomics is the study of genetic variations among individuals to predict the probability that a patient will respond to single or multidrug chemotherapy. breast cancer is one of the most common cancers among women worldwide. treatment of breast cancer by application of biological rationales gives us the ability to match the correct pharmacology to individual tumour genetic p...

2011
Lennart Hilbert

Background: Acceleration of adaptation dynamics by stress-induced hypermutation has been found experimentally. Evolved evolvability is a prominent explanation. We investigate a more generally applicable explanation by a physical constraint. Methods and Results: A generic thermodynamical analysis of genetic information storage obviates physical constraints on the integrity of genetic information...

Journal: :iranian journal of medical sciences 0
majid fardaei department of genetics, school of medicine, shiraz university of medical sciences faezeh ghaderi department of pediatric dentistry, school of dentistry, shiraz university of medical sciences, shiraz, iran somaye hekmat department of pediatric dentistry, school of dentistry, shiraz university of medical sciences, shiraz, iran reza ghaderi department of dermatology, school of medicine, birjand university of medical sciences, birjand, iran

the witkop syndrome is a rare autosomal dominant disorder characterized by the absence of several teeth and abnormalities of the nails. this is the first report of a rare genetic tooth and nail syndrome diagnosed in a 2.5-year-old boy with early exfoliation of the primary canine, absence of the primary incisors, and nail dysplasia. a homozygous mutation was identified in 3’-utr of msx1 gene in ...

Journal: :physiology and pharmacology 0
pedram torabian student research committee, golestan university of medical sciences, gorgan, iran ayyoob khosravi student research committee, golestan university of medical sciences, gorgan, iran mehdi gholizadeh student research committee, golestan university of medical sciences, gorgan, iran mehdi zahedi ischemic disorders research center, golestan university of medical sciences, gorgan, iran majid haghjoo shahid rajaei cardiovascular, medical and research center echocardiography research center, tehran university of medical sciences, tehran, iran morteza oladnabi department of human genetics, school of advanced technologies in medicine, golestan university of medical sciences, gorgan, iran

introduction: congenital long qt syndrome (lqts) is a cardiac disorder characterized by qt interval prolongation at basal ecg. different lqts genes encode ion channel subunits or proteins involved in regulating cardiac ionic currents. long qt syndrome type 6 (lqt6) is caused by mutation in the kcne2 gene. our research aimed to analyze genetic variants of kcne2 gene causing the disease in irania...

Journal: :Endocrine-related cancer 2005
M Xing

Genetic alteration is the driving force for thyroid tumorigenesis and progression, based upon which novel approaches to the management of thyroid cancer can be developed. A recent important genetic finding in thyroid cancer is the oncogenic T1799A transversion mutation of BRAF (the gene for the B-type Raf kinase, BRAF). Since the initial report of this mutation in thyroid cancer 2 years ago, ra...

Journal: :Jurnal Teknik Pertanian 2023

Genetic variation is needed for developing new superior varieties in plant breeding. of chili plants could be increased by inducing mutation with gamma rays irradiation. The aim this study was to determine radiosensitivity two local pepper calculating the lethal dose values at LD20 and LD50. Chili (Capsicum frutescens L.) seeds origin from Tulungagung Ponorogo were irradiated cobalt-60 doses of...

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